US10124024B2 - Ionizing irradiation sterilization of bacterial minicell-based biopharmaceuticals and methods of use - Google Patents

Ionizing irradiation sterilization of bacterial minicell-based biopharmaceuticals and methods of use Download PDF

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US10124024B2
US10124024B2 US15/887,432 US201815887432A US10124024B2 US 10124024 B2 US10124024 B2 US 10124024B2 US 201815887432 A US201815887432 A US 201815887432A US 10124024 B2 US10124024 B2 US 10124024B2
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minicells
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bacterial
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US20180153942A1 (en
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Matthew J. Giacalone
Gary H. Ward
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Vaxiion Therapeutics LLC
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66—Microorganisms or materials therefrom
    • A61K35/74—Bacteria
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K41/00—Medicinal preparations obtained by treating materials with wave energy or particle radiation ; Therapies using these preparations
    • A61K41/10—Inactivation or decontamination of a medicinal preparation prior to administration to an animal or a person
    • A61K41/17—Inactivation or decontamination of a medicinal preparation prior to administration to an animal or a person by ultraviolet [UV] or infrared [IR] light, X-rays or gamma rays
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/0005—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts
    • A61L2/0011—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts using physical methods
    • A61L2/0029—Radiation
    • A61L2/0035—Gamma radiation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C07K14/24—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Enterobacteriaceae (F), e.g. Citrobacter, Serratia, Proteus, Providencia, Morganella, Yersinia
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C07K14/33—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Clostridium (G)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
    • A61L2202/20—Targets to be treated
    • A61L2202/21—Pharmaceuticals, e.g. medicaments, artificial body parts
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
    • Y02A50/475—

Definitions

  • the present application is drawn to compositions and methods for the production, purification, formulation, and terminal sterilization of eubacterial minicells for use as diagnostic, therapeutic, and prophylactic biopharmaceutical products and agents for the detection, treatment, and prevention of cancer, genetic disorders, infectious disease, and other maladies.
  • Bacterial minicells are spherical nano-sized (about 400 nm) particles that can be generated from recombinant minicell-producing bacterial strains. Minicells contain all of the components and molecular constituents of their parental bacteria with the exception of the bacterial chromosome. As a result, minicells are not living, cannot replicate, and are non-infectious, making them highly suitable as in vivo delivery vehicles and vaccines with no risk of infection.
  • minicells are derived from bacterial strains that are highly amenable to recombinant engineering, recombinant expression techniques, and facile molecular biological techniques, they too are highly amenable to recombinant engineering and compared to other nanodelivery technologies, are easily converted into targeted drug delivery and vaccine vehicles.
  • a method of producing terminally sterilizing bacterial minicells intended for pharmaceutical use comprising exposing a composition comprising a plurality of bacterial minicells to ionizing irradiation.
  • the ionizing irradiation can be, for example, gamma irradiation, E-beam (electron beam, beta irradiation) irradiation, X-ray (photon) irradiation, and UV irradiation.
  • One of the preferred types of ionizing irradiation is gamma irradiation.
  • the ionizing irradiation is at a dose of about 5 kGy to about 40 kGy.
  • the ionizing irradiation is at a dose of about 25 kGy. In some embodiments, the dose of the gamma irradiation is sufficient to sterilize the composition to a level conforming to USP ⁇ 71> standards under version USP 38 NF 33.
  • the composition is a pharmaceutical composition comprising said bacterial minicells and a pharmaceutically acceptable excipient.
  • the method comprises producing a pharmaceutical composition comprising said bacterial minicells and a pharmaceutically acceptable excipient.
  • pharmaceutically acceptable excipient is trehalose.
  • the composition is a pharmaceutical composition comprising said bacterial minicells and a pharmaceutically acceptable diluent.
  • the method comprises producing a pharmaceutical composition comprising said bacterial minicells and a pharmaceutically acceptable diluent.
  • the pharmaceutically acceptable diluent is sterile water.
  • the bacterial minicells are exposed to a terminally sterilizing dose of ionizing irradiation as a frozen suspension. In some embodiments, the composition is exposed to a terminally sterilizing dose of ionizing irradiation as a frozen suspension. In some embodiments, the bacterial minicells are exposed to a terminally sterilizing dose of ionizing irradiation as a frozen lyophile. In some embodiments, the composition is exposed to a terminally sterilizing dose of ionizing irradiation as a frozen lyophile.
  • the bacterial minicells express and/or display invasin or a functional equivalent thereof.
  • the invasin can be, for example, an invasin from Yersinia pseudotuberculosis .
  • the bacterial minicells comprise perfringolysin O (PFO).
  • a pharmaceutical composition comprising a plurality of bacterial minicells, wherein said bacterial minicells have been exposed to ionizing irradiation.
  • the pharmaceutical composition is sterile.
  • the bacterial minicells or the pharmaceutical composition has been terminally sterilized.
  • the pharmaceutical composition has been exposed to ionizing irradiation.
  • the bacterial minicells comprise targeted therapeutic minicells. In some embodiments, the bacterial minicells comprise immunodulatory minicells. In some embodiments, the bacterial minicells comprise immunogenic minicells. In some embodiments, the bacterial minicells are derived from a bacterium from the genus Escherichia spp., Salmonella spp., Listeria spp., Pseudomonas spp., Acinetobacter spp., Neiserria spp., Shigella spp., Bacillus spp., or Haemophilus spp.
  • the pharmaceutical composition further comprises a pharmaceutically acceptable excipient.
  • the pharmaceutically acceptable excipient can be, for example, trehalose.
  • the pharmaceutical composition further comprises a pharmaceutically acceptable diluent.
  • the pharmaceutically acceptable diluent can be, for example, sterile water.
  • viable microbial contaminants in the pharmaceutical composition are at a level conforming to USP ⁇ 71> standards under version USP 38 NF 33.
  • the bacterial minicells express and/or display invasin or a functional equivalent thereof.
  • the invasin can be an invasin from Yersinia pseudotuberculosis .
  • the bacterial minicells comprise perfringolysin O (PFO).
  • the pharmaceutical composition is in the form of a frozen suspension. In some embodiments, the pharmaceutically composition is in the form of a frozen lyophile.
  • biopharmaceutical composition which comprises a plurality of bacterial minicells that have been exposed to a sterilizing dose of ionizing gamma irradiation.
  • the biopharmaceutical composition is sterile within the meaning of US Pharmacopeia ⁇ 71>, and wherein the bacterial cells (1) express and/or display invasin on the minicell surface, and (ii) comprise perfringolysin O as a bioactive payload, the activity of which is not affected by exposure to a sterilizing dose of gamma irradiation
  • FIG. 1 is a schematic illustration of non-limiting exemplary types of bi-specific antibodies and bi-specific anti-body derivatives that are suitable for use in the embodiments described herein.
  • FIGS. 2A-B show VAX014 minicell containing vials (frozen suspension or frozen lyophile) that have been exposed to increasing doses of gamma irradiation.
  • FIG. 3 shows reconstituted lyophilized VAX014 minicells and thawed frozen suspension of VAX014 minicells that have been exposed to increasing doses of gamma irradiation after removal from the container for visual inspection.
  • FIG. 4 shows hemolytic activity (i.e., perfringolysin O activity) in VAX014 minicell frozen suspension and frozen lyophiles after being exposed to increasing amounts of ionizing gamma irradiation.
  • FIGS. 5A-B are plots of VAX014 minicell-mediated cell-killing activity (potency) of VAX014 minicell frozen suspension or frozen lyophiles after being exposed to increasing amounts of ionizing gamma irradiation.
  • FIG. 6 is a Kaplan-Meier survival curve demonstrating no loss in VAX014 anti-tumor activity following sterilization at 25 kGy in the MB49 syngeneic orthotopic murine model of bladder cancer after intravesical administration to tumor bearing mice as compared to pre-sterilized non-irradiated VAX014.
  • FIGS. 7A-F show no loss of stability, integrity, or potency of minicells after gamma irradiation at 25 kGy, where the minicells comprise doxorubicin and display an antibody against human Epidermal Growth Factor Receptor 1 (EGFR-1) on their surfaces.
  • EGFR-1 Epidermal Growth Factor Receptor 1
  • FIGS. 8A-B show no loss of stability or integrity of minicells after gamma irradiation at 25 kGy, where the minicells comprise a recombinant expression plasmid and display an antibody against human Epidermal Growth Factor Receptor 1 (EGFR-1) on their surfaces.
  • EGFR-1 Epidermal Growth Factor Receptor 1
  • immunomodulatory minicells refers to minicells that are capable of activating, de-activating, or influencing the immune system in such a way as to be beneficial or therapeutic to a mammalian recipient suffering from disease.
  • immunological minicells refers to minicells that are capable of stimulating an adaptive immune response against a particular antigen, antigens, pathogenic organism, opportunistic organism, parasitic organism, or cancer cells (i.e. a vaccine).
  • immunotherapy refers to the use of an immunomodulatory compound, preferably an immunomodulatory minicell, to generate, enhance, impede, or otherwise influence an immune response, the result of which has a beneficial effect with respect to the elimination or slowing the progression of disease, especially cancer.
  • the term “adherent minicell” refers to a minicell that is capable of binding and adhering to the surface of a non-constitutively phagocytic eukaryotic cell without stimulating appreciable endocytosis of said minicells.
  • muco-adherent minicell refers to a minicell that is capable of binding and adhering to a mucosal surface.
  • targeted minicells refers to minicells that have been modified, for example via recombinant engineering and/or the addition of exogenous targeting moieties (e.g. antibodies and antibody derivatives), to selectively target specific tissues, organs, and/or cells.
  • exogenous targeting moieties e.g. antibodies and antibody derivatives
  • targeted therapeutic minicells refers to minicells that have been modified, for example, either via recombinant engineering and/or the addition of exogenous targeting moieties (e.g. antibodies and antibody derivatives), to selectively target specific tissues, organs, and/or cells and further contain small molecule drugs, therapeutic nucleic acids, therapeutic polypeptides, and any combination of the preceding.
  • exogenous targeting moieties e.g. antibodies and antibody derivatives
  • the term “targeted minicell vaccine” refers to bacterial minicells that encapsulate a protein antigen and/or a nucleic acid-based vaccine (e.g. DNA or RNA-based vaccine) derived from an infectious disease agent or from a tumor cell of choice, wherein the minicell further expresses and/or displays targeting moieties conferring specificity for antigen presenting cells of the immune system on the surface (e.g., external surface) of said minicells in such a way that they are able to specifically bind to, are bound by, or in some other way specifically recognize and thereby deliver, localize to, or aggregate within antigen presenting cells, organs, or tissue types involved in the genesis, progression, and/or maintenance of a recipient host immune response, to deliver the antigenic contents of the minicell to the antigen presenting target cell, tissue, and organ type in vitro or in vivo.
  • a targeted minicell vaccine may also comprise recombinant chemokines, cytokines, or interleuk
  • homotypic minicell vaccine refers to bacterial minicells produced by a pathogenic bacterium, such that the minicell vaccine is protective against said pathogenic bacterium.
  • a homotypic minicell vaccine may further comprise a protein antigen and/or a nucleic acid-based vaccine (e.g. DNA or RNA-based vaccine) derived from the same infectious disease agent.
  • a homotypic minicell vaccine may also comprise recombinant chemokines, cytokines, or interleukin proteins and functional nucleic acids encoding for the same.
  • a homotypic minicell vaccine may also be a targeted minicell vaccine.
  • Integrin-targeted minicells refers to minicells that express and/or display invasin (for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis ) and any functional equivalents thereof.
  • the term “Integrin-targeted therapeutic minicells” refers to minicells that express and/or display invasin (for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis ) and any functional equivalents thereof, wherein the minicells further comprise one or more bioactive molecules including but not limited to therapeutic polypeptides, small molecule drugs, therapeutic nucleic acids, and any combination of the preceding.
  • the term “Integrin-targeted immunomodulatory minicells” refers to minicells that express and/or display invasin (for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis ) and any functional equivalents thereof, wherein the minicells further comprise one or more bioactive molecules including but not limited to immunomodulatory polypeptides, small molecule drugs, immunomodulatory nucleic acids, and any combination of the preceding.
  • VAX-IP minicells refers to minicells that express and/or display invasin (for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis ) and any functional equivalents thereof, wherein the minicells further comprise perfringolysin O (PFO).
  • invasin for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis
  • PFO perfringolysin O
  • VAX014 minicells refers to VAX-IP minicells that have been formulated in a pharmaceutical composition which comprises sterile D-trehalose as an excipient.
  • VAX-IPT minicells refers to minicells that express and/or display invasin (for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis ) and any functional equivalents thereof, wherein the minicells further comprise perfringolysin O (PFO) and a protein toxin.
  • invasin for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis
  • PFO perfringolysin O
  • VAX-IPP minicells refers to minicells that express and/or display invasin (for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis ) and any functional equivalents thereof, wherein the minicells comprise perfringolysin O (PFO) and an exogenous polypeptide other than a protein toxin.
  • invasin for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis
  • PFO perfringolysin O
  • VAX-IPD minicells refers to minicells that express and/or display invasin (for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis ) and any functional equivalents thereof, wherein the minicells comprise perfringolysin O (PFO) and a catalytic fragment of diphtheria toxin.
  • invasin for example, the pan-Beta1-integrin-targeting cell surface molecule Invasin from Yersinia pseudotuberculosis
  • PFO perfringolysin O
  • prokaryotic cell division gene refers to a gene that encodes a gene product that participates in the prokaryotic cell division process.
  • Many cell division genes have been discovered and characterized in the art. Examples of cell division genes include, but are not limited to, zipA, sulA, secA, dicA, dicB, dicC, dicF, ftsA, ftsI, ftsN, ftsK, ftsL, ftsQ, ftsW, ftsZ, minC, minD, minE, seqA, ccdB, sfiC, and ddlB.
  • the term “transgene” refers to a gene or genetic material that has been transferred naturally or by any genetic engineering techniques from one organism to another.
  • the transgene is a segment of DNA containing a gene sequence that has been isolated from one organism and is introduced into a different organism. This non-native segment of DNA may retain the ability to produce RNA and/or protein in the transgenic organism, or it may alter the normal function of the transgenic organism's genetic code.
  • the transgene is an artificially constructed DNA sequence, regardless of whether it contains a gene coding sequence, which is introduced into an organism in which the transgene was previously not found.
  • an agent is said to have been “purified” if its concentration is increased, and/or the concentration of one or more undesirable contaminants is decreased, in a composition relative to the composition from which the agent has been purified.
  • purification includes enrichment of an agent in a composition and/or isolation of an agent therefrom.
  • sufficiently devoid of viable parental cells synonymous with “sufficiently devoid”, as used herein refers to a composition of purified minicells that have a viable parental cell contamination level that has little or no effect on the toxicity profile and/or therapeutic effect of targeted therapeutic minicells.
  • sterilized means to be sufficiently devoid of bioburden as to satisfy the requirements under the standard Sterility Testing ⁇ 71> of the United States Pharmacopeia version USP 38 NF 33, its harmonized foreign counter parts, and other approved international pharmaceutical standards.
  • terminal sterilized refers to the final step in a drug manufacturing process wherein the final drug product is found to be sufficiently devoid of bioburden as to satisfy the requirements under the standard Sterility Testing ⁇ 71> of the United States Pharmacopeia version USP 38 NF 33, its harmonized foreign counter parts, and other approved international pharmaceutical standards.
  • a terminally sterilized drug product can be ready for administration to a subject.
  • domain refers to a region of a molecule or structure that shares common physical and/or chemical features.
  • Non-limiting examples of protein domains include hydrophobic transmembrane or peripheral membrane binding regions, globular enzymatic or receptor regions, protein-protein interaction domains, and/or nucleic acid binding domains.
  • prokaryotic used herein encompasses, for example, Eubacteria, including both Gram-negative and Gram-positive bacteria, prokaryotic viruses (e.g., bacteriophage), and obligate intracellular parasites (e.g., Richettsia, Chlamydia , etc.).
  • immunomodulatory polypeptide refers to any collection of diverse protein molecule types that have an immunomodulatory effect when introduced into a eukaryotic organism or cell (e.g., a mammal such as human).
  • An immunomodulatory polypeptide can be a cytokine, a chemokine, a cholesterol-dependent cytolysin, a functional enzyme, an antibody or antibody mimetic, an activated caspase, a pro-caspase, a cytokine, a chemokine, a cell-penetrating peptide, or any combination and/or plurality of the proceeding.
  • the term should not be confused with the word “immunogen” or “antigen”, each of which is described below.
  • immunomodulatory responses are interchangeable and used herein to refer to polypeptides, carbohydrates, lipids, nucleic acids, and other molecules to which an antigen-specific antibody, cellular, and/or allergenic response may be mounted against.
  • Antigen-specific immune responses shall rely on the presence of the antigen/immunogen, and shall not be included in the definition of immunomodulatory responses as used herein.
  • overexpression refers to the expression of a functional nucleic acid, polypeptide or protein encoded by DNA in a host cell, wherein the nucleic acid, polypeptide or protein is either not normally present in the host cell, or wherein the nucleic acid, polypeptide or protein is present in the host cell at a higher level than that normally expressed from the endogenous gene encoding the nucleic acid, polypeptide or protein.
  • modulate means to interact with a target either directly or indirectly so as to alter the activity of the target to regulate a biological process.
  • the mode of “modulate” includes, but is not limited to, enhancing the activity of the target, inhibiting the activity of the target, limiting the activity of the target, extending the activity of the target, and attenuating the activity of the target.
  • heterologous refers to a protein, gene, nucleic acid, imaging agent, buffer component, or any other biologically active material that is not naturally found in a minicell or minicell-producing bacterial strain (for example, has been recombinantly introduced or transformed into the minicell-producing parent cell) that is expressed, transcribed, translated, amplified or otherwise generated by minicell-producing bacterial strains that harbor recombinant genetic material coding for said heterologous material or coding for genes that are capable of producing said heterologous material (e.g., a bioactive metabolite not native to the parent cell).
  • exogenous refers to a protein (e.g., antibodies), gene(s), nucleic acid(s), small molecule drug(s), imaging agent(s), buffer, radionuclide(s), or any other biologically active or inactive material that is not native to a cell, or in the case of a minicell, not native to the parent cell of the minicell (for example, has been recombinantly introduced or transformed into the minicell-producing parent cell).
  • Exogenous material differs from heterologous material by virtue of the fact that it is generated, purified, and added separately.
  • terapéutica as used herein means having a biological effect or combination of biological effects that inhibits, eliminates, reduces, or prevents progression of a disease or other aberrant biological processes in an animal (including humans).
  • prophylactic means having a biological effect or combination of biological effects that prevents or delays progression or establishment of a disease, disease state, or other aberrant biological processes in an animal (including humans).
  • diagnosis means having the ability to detect, monitor, follow, and/or identify a disease or condition in an animal (including humans) or from a biological sample including but not limited to blood, urine, saliva, sweat and fecal matters.
  • theranostic means having the combined effects of a therapeutic and a diagnostic composition.
  • nucleic acid(s) and/or protein(s) means the expression of one or more nucleic acid(s) and/or protein(s) from a nucleic acid molecule that is artificially constructed using modern genetic engineering techniques wherein the artificially constructed nucleic acid molecule does not occur naturally in minicells and/or minicell-producing bacterial strains wherein the artificial nucleic acid molecule is present as an episomal nucleic acid molecule or as part of the minicell-producing bacterial chromosome.
  • episomal refers to a nucleic acid molecule that is independent of the chromosome(s) of a given organism or cell.
  • detoxified refers to a modification made to a composition or component thereof that results in a significant reduction in acute toxicity to the modified composition or component thereof, regardless of what the causative biological basis for toxicity to the composition or component thereof happens to be.
  • bioactive molecule refers to a molecule having a biological effect on an eukaryotic organism or cell (e.g., a mammal such as human) when introduced into the eukaryotic organism or cell.
  • bioactive molecules include, but are not limited to, therapeutic nucleic acids, therapeutic polypeptides (including protein toxins), and therapeutic small molecule drugs.
  • the present disclosure relates to the generation and use of terminally sterilized bacterial minicell-based compositions in vitro and in vivo for the targeted delivery of small molecule drugs, nucleic acids, polypeptides, and imaging agents to different tissues, organs, and cell types with intended use as medicaments in the treatment and prevention of cancer, infectious disease, autoimmune disease, genetic disorders, and other biological maladies in higher order animals including but not limited to those found in the phylum Chordata.
  • compositions and methods for the production of bacterial minicell-based pharmaceutical, diagnostic, and vaccine products where ionizing irradiation, for example high-dose ionizing irradiation, is employed to sterilize the product.
  • ionizing irradiation for example high-dose ionizing irradiation
  • the methods disclosed herein remove viable contaminating parental cells and other adventitious microbes while ensuring sterility, using fewer steps and eliminating the need for the addition of additional antibiotics or hypertonic conditions, while preserving minicell integrity, stability, and product function.
  • Bacterial minicells are achromosomal, membrane-encapsulated biological nanoparticles (approximately 250-500 nm in diameter) that are formed by bacteria following a disruption in the normal division apparatus of bacterial cells.
  • minicells are small, metabolically active replicas of normal bacterial cells with the exception of chromosomal DNA and as such, are non-dividing, non-viable, and non-infectious.
  • Bacterial minicells may be generated from a wide variety of Gram-negative and Gram-positive species and strains of bacteria including but not limited to Escherichia spp, Salmonella spp., Pseudomonas spp., Listeria spp., Burkholderia , spp., Shigella spp., Bacillus spp., Acinetobacter spp., Franciscella spp. Legionella spp., Lactobacillus spp., Clostridium spp., Campylobacter spp., Neisseria spp., Chlamydia spp., and the like.
  • minicells can be “engineered” to preferentially encapsulate, be coupled to, or absorb biologically active molecules, including but not limited to nucleic acids, proteins, small molecule drugs, and any combination thereof for subsequent delivery and generation of responses in both prophylactic and therapeutic medicinal applications where the prevention, maintenance, and/or inhibition of disease is desirable.
  • biologically active molecules including but not limited to nucleic acids, proteins, small molecule drugs, and any combination thereof for subsequent delivery and generation of responses in both prophylactic and therapeutic medicinal applications where the prevention, maintenance, and/or inhibition of disease is desirable.
  • 7,611,885 described a method combining (i) differential centrifugation, (ii) two rounds of density gradient purification, (iii) cross-flow filtration through a 0.45 uM filter, (iv) treatment with a high concentration of salt to induce osmotic shock resulting in parent cell filamentation, (v) treatment with an antibiotic (vi) cross-flow filtration through a 0.2 uM filter, (vii) cross-flow filtration through a second 0.45 uM, (viii) concentration of minicells through a 100 kDa filter, (ix) treatment with anti-endotoxin antibodies couple to magnetic beads, (x) magnetic separation of endotoxin bound to said beads, (xi) collection of minicells, and then presumably (xii) formulation into excipient or other vehicle for final API generation.
  • the present disclosure impinges on the unexpected finding that bacterial minicells can be terminally sterilized by exposure to ionizing irradiation, for example high dose ionizing irradiation, with no loss of potency, targeting ability, or stability while achieving the benefit of complete elimination of contaminating viable parental cells.
  • This finding allows for the use of more scalable, conventional, GMP-compatible/compliant minicell purification methodologies while allowing a mechanism by which to terminally sterilize bacterial minicell-based biopharmaceutical products to a level sufficient to satisfy Sterility Testing standards under USP ⁇ 71> version USP 38 NF 33 and its harmonized foreign equivalents.
  • ionizing irradiation is capable of achieving sterility, as it is the sterilization methodology of choice for medical device and surgical instrument products.
  • ionizing irradiation works by generating free oxygen radicals. Free oxygen radicals are a highly reactive molecular species that quickly introduce breaks in the covalent bonds of nucleic acids and proteins, leading to cell and/or microbe death.
  • Free oxygen radicals are a highly reactive molecular species that quickly introduce breaks in the covalent bonds of nucleic acids and proteins, leading to cell and/or microbe death.
  • sterility applications it is commonly held that a dose of 5 kGy is sufficient to terminally sterilize, although more often than not a higher dose of 25 kGy is used to ensure sterility and complete absence of viable microbial growth.
  • isolated proteins or protein mixtures that are exposed to ionizing irradiation are also quickly rendered inactive.
  • the methods described in the present disclosure goes against what is known about the effects of ionizing irradiation on biomaterials and bacteria containing functional proteins, and as demonstrated herein that bacterial minicells and bacterial minicell-based biopharmaceutical products can be terminally sterilized by exposure to ionizing irradiation with no loss of integrity, specificity, stability, potency, and in vivo activity while eliminating all viable contaminating parental cells and/or adventitious microbes.
  • the minicells disclosed herein are derived from minicell-producing strains that comprise one or more of the three safety features disclosed below.
  • the minicell-producing strains comprise one or more of these three synergistic safety features.
  • the minicell-producing strain can comprise one, two, or all of these three safety features. The first is a genetic suicide mechanism that kills residual live parental cells without lysing them (and expelling free lipopolysaccharide) after the minicell formation step has been completed.
  • the present application incorporates the use of a regulated genetic suicide mechanism that upon exposure to the appropriate inducer, introduces irreparable damage to the chromosomes of minicell-producing parental cells as described in US2010-0112670, incorporated by reference herein.
  • the suicide mechanism operates to introduce irreparable double-stranded breaks to the chromosome of the parental cells and can be used as an adjunct to conventional separation techniques to improve minicell purification.
  • the second safety feature is a defined auxotrophy, preferably but not necessarily in the diaminopimelic acid (DAP) biosynthesis pathway, and most preferably in the dapA gene of an E. coli minicell-producing strain.
  • DAP diaminopimelic acid
  • the third safety feature entails a deletion of the lpxM gene in E. coli minicell-producing strains. Deletion of the lpxM gene can result in the production of de-toxified lipopolysaccharide (LPS) molecules.
  • LPS lipopolysaccharide
  • the lpxM gene (also referred to as the msbB gene) functions to add a terminal myristolic acid group to the lipid A portion of the LPS molecule and removal of this group (by way of elimination of the lpxM gene) results in marked detoxification of LPS. Specifically, detoxification is characterized by a decrease in the production of pro-inflammatory cytokines in response to exposure to LPS.
  • this modification does not teach away from the present invention with respect to immunomodulatory minicell compositions as cytokine production in response to the detoxified form of LPS can still occur, albeit not at the same level as wildtype LPS.
  • the detoxification controls only the levels of cytokines produced, making it possible to dampen the acute sepsis-like pro-inflammatory response while allowing more robust Th1 and/or Th2 immune responses, to be achieved without overt toxicity.
  • This deletion can be introduced into any functionally equivalent gene of any Gram-negative or Gram-positive minicell-producing strain to achieve the same effect.
  • the enhanced safety profile can reduce the risk of and potential for developing sepsis. From a regulatory and manufacturing perspective, it is also preferred that antibiotic resistance markers be eliminated from the bacterial chromosome of the minicell-producing parental cell strain.
  • One or more of the safety features can be optional.
  • minicell formation is induced by the presence of one or more chemical compounds selected from isopropyl ⁇ -D-1-thiogalactopyranoside (IPTG), rhamnose, arabinose, xylose, fructose, melibiose, and tetracycline.
  • IPTG isopropyl ⁇ -D-1-thiogalactopyranoside
  • rhamnose arabinose
  • xylose fructose
  • fructose melibiose
  • tetracycline tetracycline.
  • the expression of the gene encoding the genetic suicide endonuclease is induced by a change in temperature.
  • the method further comprises purifying the immunomodulatory minicells from the composition.
  • immunomodulatory minicells are terminally sterilized by exposure to ionizing irradiation. In some embodiments, immunomodulatory minicells are terminally sterilized by exposure to ionizing gamma irradiation.
  • minicell formation is induced by the presence of one or more chemical compounds selected from isopropyl ⁇ -D-1-thiogalactopyranoside (IPTG), rhamnose, arabinose, xylose, fructose, melibiose, and tetracycline.
  • IPTG isopropyl ⁇ -D-1-thiogalactopyranoside
  • rhamnose arabinose
  • xylose fructose
  • fructose melibiose
  • tetracycline tetracycline.
  • the expression of the gene encoding the genetic suicide endonuclease is induced by a change in temperature.
  • the method further comprises purifying the immunogenic minicells from the composition.
  • the immunogenic minicells are substantially separated from the parent cells by a process selected from the group including but not limited to centrifugation, filtration, ultrafiltration, ultracentrifugation, density gradient(s), immunoaffinity, immunoprecipitation, and any combination of the preceding purification methods.
  • immunogenic minicells are lyophilized.
  • immunogenic minicells are frozen.
  • immunogenic minicells are lyophilized and then frozen.
  • immunogenic minicells are formulated as a frozen suspension in a cryoprotectant excipient or other pharmaceutically acceptable carrier or GRAS substance.
  • immunogenic minicells are exposed to ionizing irradiation.
  • immunogenic minicells are terminally sterilized by exposure to ionizing irradiation.
  • immunogenic minicells are terminally sterilized by exposure to ionizing gamma irradiation.
  • Some embodiments provide a method of making targeted therapeutic minicells, comprising culturing the targeted therapeutic minicell-producing bacteria disclosed herein and substantially separating targeted therapeutic minicells from the minicell-producing parent cells, thereby generating a composition comprising targeted therapeutic minicells.
  • the method further comprises inducing targeted therapeutic minicell formation from a culture of minicell-producing parent cells.
  • the method further comprises inducing expression of the gene encoding the genetic suicide endonuclease.
  • targeted therapeutic minicell formation is induced by the presence of one or more chemical compounds selected from isopropyl ⁇ -D-1-thiogalactopyranoside (IPTG), rhamnose, arabinose, xylose, fructose, melibiose, and tetracycline.
  • IPTG isopropyl ⁇ -D-1-thiogalactopyranoside
  • rhamnose arabinose
  • xylose fructose
  • fructose melibiose
  • tetracycline tetracycline.
  • the expression of the gene encoding the genetic suicide endonuclease is induced by a change in temperature.
  • the method further comprises purifying the targeted therapeutic minicells from the composition.
  • the targeted therapeutic minicells are substantially separated from the parent cells by a process selected from the group including but not limited to centrifugation, filtration, ultrafiltration, ultracentrifugation, density gradient(s), immunoaffinity, immunoprecipitation, and any combination of the preceding purification methods.
  • targeted therapeutic minicells are lyophilized.
  • targeted therapeutic minicells are frozen.
  • targeted therapeutic minicells are lyophilized and then frozen.
  • targeted therapeutic minicells are formulated as a frozen suspension in a cryoprotectant excipient or other pharmaceutically acceptable carrier or GRAS substance.
  • targeted therapeutic minicells are exposed to ionizing irradiation.
  • targeted therapeutic minicells are terminally sterilized by exposure to ionizing irradiation.
  • targeted therapeutic minicells are terminally sterilized by exposure to ionizing gamma irradiation.
  • Minicells are achromosomal, membrane-encapsulated biological nanoparticles (approximately 250-500 nm in diameter depending on the strain type and growth conditions used) that are formed by bacteria following a disruption in the normal cell division apparatus.
  • minicells are small, metabolically active replicas of normal bacterial cells with the exception that they contain no chromosomal DNA and as such, are non-dividing and non-viable.
  • minicells do not contain chromosomal DNA, plasmid DNA, RNA, native and/or recombinantly expressed proteins, and other metabolites have all been shown to segregate into minicells.
  • minicell production can be achieved by the over-expression or mutation of genes involved in the segregation of nascent chromosomes into daughter cells. For example, mutations in the parC or mukB loci of E. coli have been demonstrated to produce minicells. Both affect separate requisite steps in the chromosome segregation process in Enterobacteriacea. It can be assumed that like the cell division genes described above, manipulation of wild type levels of any given gene involved in the chromosome segregation process that result in minicell production will have similar effects in other family members.
  • minicell producing strains of the family Enterobacteriacea For example, deletion of the min locus in any of Enterobacteriacea family members results in minicell production.
  • Cell division genes from the Enterobacteriacea in which mutation can lead to minicell formation include but are not limited to the min genes (MinCDE). While minicell production from the min mutant strains is possible, these strains have limited commercial value in terms of being production strains for minicell-based biopharmaceuticals. Strains with deletions or mutations within the min genes make minicells at constitutively low levels, presenting problems in terms of commercialization and economies of scale as well as severely limiting the use of recombinant expression technology to generate the bioactive molecules intended for delivery.
  • Minicell yields from the min mutant strains are relatively low, which can increase production cost and/or scale required to generate sufficient numbers of minicells to support market demand for a given biopharmaceutical.
  • deletion(s) in the min locus impart constant selective pressure on these strains and the spontaneous generation of compensatory suppressor mutations can lead to a loss of minicell-producing phenotype. This eventuality can have potential negative impact upon minicell yield.
  • using cell division mutant strains to produce minicells that encapsulate biologically active molecules that are recombinantly expressed by the minicell-producing parent cells (such as proteins, RNA, DNA, and other catabolites for diagnostic or therapeutic delivery) is problematic.
  • the preferred method is to induce the formation of the biologically active molecule(s) within the parental cells prior to inducing the minicell phenotype, so that all of the minicells produced will contain the desired amount of the biologically active molecule(s).
  • the minicells themselves are capable of producing the bioactive molecule after being separated from the parental cells. This includes but is not limited to forming the bioactive molecule from an episomal nucleic acid or RNA encoding for the bioactive molecule located within the minicell or by preexisting protein constituents of minicells after being separated from the parental cells. Any of these expression strategies can be employed to express and/or display binding moieties on the surfaces of minicells. These advantages, when used in combination, result in a higher quality and quantity of minicells.
  • these minicells can further comprise small molecule drugs that can be loaded into minicells as described in more detail below.
  • live parental cells have been eliminated through either physical means or biological means or both.
  • Physical means include the use of centrifugation-based separation procedures, filtration methodologies, chromatography methodologies, or any combination thereof.
  • Biological elimination is achieved by but not limited to the preferential lysis of parental cells, the use of auxotrophic parental strains, treatment with antibiotics, treatment with UV irradiation, essential metabolite deprivation including but not limited to diaminopimelic acid (DAP) deprivation, selective adsorption of parental cells, treatment with other DNA damaging agents, and induction of a suicide gene.
  • DAP diaminopimelic acid
  • Diaminopimelic acid (DAP) deprivation can be useful in the elimination of live parental cells with the exception that this approach is limited by the number of species it can be used for. In other words, not all parent cell species capable of producing minicells require DAP for survival. DAP mutants in E. coli minicell-producing strains are of great advantage and in some cases preferred over the wild type.
  • the advantage of using DAP is that this compound (diaminopimelic acid, an E. coli cell wall constituent) is critical for the growth of E. coli and is not present in or produced by animals. Thus, should a “viable” E.
  • coli minicell-producing parental cell be administered along with targeted minicells, the parental cell will be unable to grow and will thereby be inert to the animal and with respect to minicell activity.
  • a similar approach can be used with Salmonella spp. based minicell-producing parental strains except in that case the aro genes, preferably aroB are removed.
  • Selective adsorption methodologies have yet to be explored with respect to purifying minicells from viable parental cells.
  • Selective adsorption is defined as any process by which parental cells or minicells are preferentially adsorbed to a substrate by virtue of their affinity for the substrate.
  • high affinity protein-protein interactions could be exploited for this use.
  • the novel minicell outer membrane protein Lpp-OmpA::Protein A has a high affinity for the Fc region of most antibodies.
  • the gene encoding for Lpp-OmpA::Protein A is under the control an inducible promoter could easily be introduced on to the chromosome of a minicell producing strain.
  • Minicells could be produced from this strain prior to the activation of expression of the Lpp-OmpA::ProteinA gene such that the minicells produced do not express or display Lpp-OmpA::Protein A on their cell surface.
  • the viable cells within the culture could be given the signal to produce the Lpp-OmpA::Protein A protein such that Lpp-OmpA::Protein A is only expressed and displayed upon viable cells.
  • Lpp-OmpA::Protein A is preferentially expressed on the surface of viable parental cells, they can be easily adsorbed to a substrate coated with antibodies or other Fc-region containing proteins.
  • minicells can be selectively purified away from viable parental cells by a number of different means dependent upon the substrate type used.
  • Substrates include but are not limited to solid-phase chromatographic columns used in gravity filtration applications, magnetic beads, ion exchange columns, or HPLC columns.
  • the final composition it is advantageous for the final composition to contain few enough contaminating parental cells, viable or otherwise, so as not to be too toxic or interfere with the activity of targeted minicells when administered in vivo for therapeutic purposes.
  • Minicells can be engineered, for example, to preferentially target particular cell types through recombinant expression and minicell-surface display of cell-specific targeting moieties.
  • This approach includes the use of bacterial membrane protein fusion and display technologies as well as the expression of heterologous bacterial adhesin and other bacterial cell attachment or invasin molecules.
  • minicells are engineered to express and/or display an outer membrane protein fused to a cell targeting polypeptide such that the cell-targeting polypeptide is displayed on the minicell surface in sufficient quantities as to confer cell-specific targeting properties to said minicell.
  • Such outer membrane proteins with which cell targeting polypeptides may be fused and displayed on the minicell surface include but are not limited to Lpp-OmpA, LamB, TraA, OmpC, OmpF, FliC, FliD, IgAP, fimbrae proteins and pilus proteins.
  • Targeting polypeptides to be fused and displayed include but are not limited to single chain antibody fragments (scFv) specific for eukaryotic cell membrane proteins, eukaryotic receptor ligands (EGF, VEGF, PDGF, etc.), and non-naturally occurring targeting polypeptides arrived at through orthogonal screening technologies such as phage display.
  • scFv single chain antibody fragments
  • Minicells can be engineered to preferentially target particular cell types through the coupling of cell-specific targeting moieties onto the minicell surface using either non-covalent or covalent coupling technologies.
  • Covalent coupling technologies incorporate the use of chemical cross-linkers to attach a wide variety of targeting moieties to the surface of minicells.
  • moieties include but are not limited to polypeptides, nucleic acids, and small molecules and cross-linking reagents appropriate for each are easily selected for each moiety type by those skilled in the art.
  • Cross-linking reagents include but are not limited to those listed in Table 1.
  • Preferred targeting moieties to be covalently attached to the minicell surface include but are not limited to antibodies and antibody derivatives.
  • the targeting molecule preferably an antibody or antibody derivative
  • the targeting molecule is functionalized per the specifications provided in the cross-linker manufacturer's product insert in one reaction, while minicells to be coupled are functionalized per the manufacturer's further specifications in a separate reaction (typically a treatment with a reducing agent such as dithiothreitol, 2-beta mercaptoethanol, or tris(2-carboxyethyl)phosphine).
  • the functionalized targeting moiety and the functionalized minicells can then be mixed together, preferably at a molar ratio of greater than 1 targeting molecule to 1 minicell, and allowed to incubate to complete the coupling reaction as per the specifications in the cross-linker manufacturer's product insert(s).
  • targeted minicells following a pair of brief wash steps (e.g., pelleting minicells and resuspending targeted minicells in a buffered solution, preferably phosphate-buffered saline) targeted minicells can then be further loaded with small molecule drugs or small nucleic acid payloads by co-incubation with either or both at room temperature or 4° C. for 2-24 hours.
  • minicells following incubation, excess drug and small nucleic acids are washed away (again by pelleting and resuspending) and targeted, payload-containing minicells are formulated in a pharmaceutically acceptable excipient, preferably a GRAS substance in a pharmaceutical grade diluent.
  • a pharmaceutically acceptable excipient for example, D-trehalose in sterile water for injection
  • minicells can be placed in individual sealed, stoppered vials and stored as a frozen suspension or further lyophilized and the lyophile stored frozen. Vials containing minicells as a lyophile or frozen suspension can then be terminally sterilized by exposure to ionizing irradiation and stored frozen until use.
  • Carbodiimides (dicyclohexylcarbodiimide Used to cross-link [DCC], 1-Ethyl-3-[3- polypeptides, dimethylaminopropyl]carbodiimide peptides, DARPins, hydrochloride [EDC or EDAC]) and other amine- containing targeting molecules to exposed external regions of minicell outer membrane proteins containing exposed naturally occurring or recombinantly engineered carboxyl termini. Conversely, used to cross-link polypeptides, peptides, DARPins, and other targeting molecules via their carboxyl termini to exposed external regions of minicell outer membrane proteins containing amines.
  • Antibodies can be used to aid in the targeting of minicells to a specific tissue, organ, and cell type involved in the cause, progression, maintenance, or manifestation of disease can be derived from or be part of any immunoglobulin or immunoglobulin subclass, including but not limited to IgA, IgM, IgD, IgG, and IgE.
  • Antibodies of any subclass intended to facilitate the targeting function of minicells can be “humanized”, although any antibody of any subclass against a cell specific antigen can be raised in any animal known to generate antibody responses through adaptive immunity to achieve the same goal. In nature, antibodies are generated such that they contain two separate arms (Fab′s), each of which recognizes the same epitope of a particular antigen.
  • antibody derivatives are referred to as a ‘bispecific’ antibodies or ‘bispecific’ targeting moieties.
  • two separate antibodies can be non-covalently attached by coupling them to soluble Protein A, Protein G, or Protein A/G (or any other binding molecule that will recognize and bind two or more antibodies) to form a bispecific antibody derivative capable of adhering to the surface of minicells wherein one antibody within the complex specifically adheres to the surface of the minicell and the other antibody is displayed to specifically recognize and thereby “target” a specific cell, tissue, or organ type expressing an eukaryotic cell-specific surface antigen in vivo.
  • two separate antibodies, with separate specificities can be covalently linked using myriad cross-linking techniques to achieve the same effect.
  • Non-covalent attachment of targeting moieties includes the use of bi-specific ligands and bi-specific antibodies wherein one portion of the bi-specific ligand or bi-specific antibodies recognize the minicell surface and another portion of the bi-specific ligand or antibodies recognize a eukaryotic cell membrane protein.
  • Bi-specific antibodies and antibody derivatives are defined as those that contain one or more complementarity determining regions (CDR) specific for a minicell surface molecule and one or more CDR(s) specific for a eukaryotic cell.
  • CDR complementarity determining regions
  • Bi-specific ligands can, in some embodiments, contain one or more portions specific for the minicell surface and another specific for a eukaryotic cell.
  • One of the preferred methods of non-covalent attachment of antibodies and other ligands to minicells is described in WO/2012/112,696, which is incorporated herein in its entirety by way of reference.
  • the technology described in WO/2012/112,696 utilizes an approach of displaying an Fc-binding region of Protein A or Protein G on the minicell surface by way of a fusion protein and coupling those minicells to an Fc region-containing antibody or other polypeptide ligand to confer targeting properties to said minicells.
  • multivalent antibody derivative subtypes can be used to generate targeted minicells.
  • at least one arm of the antibody derivative(s) used is specific for one or more minicell surface structures including but not limited to porin proteins, flagella, pilus, and O-antigen, while the one or more of the additional arms is specific for one or more eukaryotic targets.
  • Bi-specific antibodies made utilizing a cross-linker (bispecific (mab) 2 and bispecific F(ab′) 2 ) are generated utilizing any of the appropriate members of those listed in FIG. 1 , especially with SPDP or any of its listed derivatives.
  • Other multivalent antibody types shown are made using established recombinant, selection, purification, and characterization techniques commonly known to the skilled artisan.
  • minicells In applications where covalent and non-covalent attachment of antibodies or other targeting moieties are utilized, it is preferable but not mandatory to first purify minicells from parental cells prior to coupling of targeting moieties. As described in more detail below, purified minicells either already contain their respective therapeutic, immunomodulatory, and immunogenic payload at the time of purification, or payloads are added to minicells following purification. In some instances, it is desirable to use a combination of both of these approaches. In the context of the latter two scenarios, targeting moieties may be added prior to or following the addition of exogenous payload(s) to minicells at the discretion of the skilled artisan. The final minicell composition is then further processed and prepared for terminal sterilization by ionizing irradiation.
  • the antibody, antibody derivative, or other targeting molecule on the surface of targeted therapeutic minicells can preferentially recognize but is not limited to recognizing cell-specific surface antigens including but are not limited to ⁇ 3 ⁇ 1 integrin, ⁇ 4 ⁇ 1 integrin, ⁇ 5 ⁇ 1 integrin, ⁇ v ⁇ 3 integrin, ⁇ v ⁇ 1 integrin, ⁇ 1 integrin, 5T4, CAIX, CD4, CD13, CD19, CD20, CD22, CD25, CD30, CD31, CD33, CD34, CD40, CD44v6, CD45, CD51, CD52, CD54, CD56, CD64, CD70, CD74, CD79, CD105, CD117, CD123, CD133, CD138, CD144, CD146, CD152, CD174, CD205, CD227, CD326, CD340, Cripto, ED-B, GD2, TMEFF2, VEGFR1, VEGFR2, FGFR, PDGFR, ANGPT1, TIE1, TIE2, N
  • the targeting moiety is selected, in part, because the binding of the minicell-surface displayed antibody targeting moiety, antibody derivatives, and/or other targeting molecules specific for the antigen induce internalization of the targeted minicell, facilitating intracellular payload delivery.
  • Previously described target-specific antibodies that are used as the targeting component include but are not limited to mAb 3F8, mAb CSL362, mAb CSL360, mAb J591, Abagovomab, Abciximab, Adalimumab, Afelimomab, Afutuzumab, Alacizumab, ALD518, Alemtuzumab, Altumomab, Anatumomab, Anrukinzumab, Apolizumab, Arcitumomab, Aselizumab, Atlizumab, Atorolimumab, Bapineuzmab, Basiliximab, Bavituximab, Bectum
  • Eubacterial minicells are capable of encapsulating and delivering several classes of biologically active compounds that have therapeutic, immunomodulatory, immunogenic, and/or diagnostic benefit to an animal, for example a mammal (e.g. a human).
  • Types of biologically active compounds (payloads) that can be delivered by minicells include but are not limited to small molecules (including small molecule drugs), nucleic acids, polypeptides, radioisotopes, lipids, lipopolysaccharides, and any combination thereof.
  • Methods of loading minicells with bioactive payloads include two categories of approaches, and these two categories of approaches may be combined. The first category of approach is by loading exogenous payload(s) into minicells via physical or chemical means. The second category of approach is the recombinant production or expression of the bioactive payload in minicells.
  • the first method of loading minicells with payload(s) is amenable to but not limited to the loading of exogenous small molecule drugs.
  • small molecule refers to a molecule that has a biological effect and that has a molecular weight of less than 5000 Daltons. In some embodiments, small molecules have a molecular weight of less than 2500 Daltons. In some embodiments, small molecules have a molecular weight of less than 1000 Daltons. In some embodiments, small molecules have a molecular weight of less than 800 Daltons. In some embodiments, small molecules have a molecular weight of less than 500 Daltons.
  • Small molecule drugs include those small molecules that result in pharmacological therapeutic benefit to an animal (including humans).
  • small molecules are loaded into minicells by incubating minicells in a high concentration of said small molecule. Over time, small molecules passively diffuse into minicells where they interact with various molecular constituents of minicells thereby becoming entrapped in minicells. Small molecules can be, in some embodiments, released by minicells into target cells once minicells are internalized into endosomes and the degradation/release process ensues.
  • the species of small molecule drug(s) compatible for use in minicells can be selected from but not limited to antibiotics (anti-infectives, anti-neoplastics, and anti-virals), anti-histamines, and anti-inflammatory pharmacological small molecule agents.
  • Antibiotics that may be used in this context include but are not limited to: (1) DNA damaging agents and agents that inhibit DNA synthesis such as anthracyclines (doxorubicin, daunorubicin, epirubicin), alkylating agents (bendamustine, busulfan, carboplatin, carmustine, cisplatin, chlorambucil, cyclophosphamide, dacarbazine, hexamethylmelamine, ifosphamide, lomustine, mechlorethamine, melphalan, mitotane, mytomycin, pipobroman, procarbazine, streptozocin, thiotepa, and triethylenemelamine), platinum derivatives (cisplatin, carboplatin, cis diamminedichloroplatinum), telomerase and topoisomerase inhibitors (Camptosar), (2) microtubule and
  • the second method of loading minicells with therapeutic, immunomodulatory, and immunogenic payloads can be via recombinant expression or production of the payload in minicells.
  • the minicell-producing parental cells can be used to recombinantly express/produce one or more therapeutic, immunomodulatory, and/or immunogenic nucleic acid molecules and/or polypeptides prior to or at the same time that minicells are being produced.
  • Recombinant nucleic acids and/or polypeptides are expressed, segregate into, and are encapsulated by minicells, then delivered to eukaryotic cells by targeted minicells in vivo or in vitro.
  • RNA interference molecule(s), or ribozyme(s) double stranded therapeutic RNA (e.g., dsRNA or siRNA), single stranded therapeutic RNA (e.g., shRNA), microRNA, long noncoding RNA, CRISPR RNA, aptamers, ribozymes, eukaryotic expression plasmids encoding for therapeutic polypeptide(s) and/or therapeutic nucleic acids, and any combination of the preceding.
  • Recombinant expression of nucleic acid(s) can be the result of expression from any of the various episomal recombinant prokaryotic expression vectors known in the art including, but not limited to plasmids, cosmids, phagemids, and bacterial artificial chromosomes (BACs), and any combination of the preceding. Recombinant expression can also be achieved by a chromosomally located prokaryotic expression cassette present in one or more copies of the minicell-producing parent cell chromosome. In cases where the nucleic acid molecule(s) to be delivered exert their effects through a “gene silencing” mechanism of action, the nucleic acids are specific for one or more different eukaryotic mRNA transcripts.
  • the nucleic acids can be delivered by the same minicell such that one or more genes are silenced by a single delivery event.
  • Targeted minicells are also used to deliver any of these nucleic acids in combination.
  • targeted minicells are used to deliver one or more small molecule drugs in concert with one or more nucleic acids.
  • the therapeutic nucleic acid molecule(s) is pre-formed by the parental cell by way of recombinant expression from a prokaryotic expression cassette (either chromosomal or episomal in location) and is then packaged inside of the minicells as double stranded RNAs (e.g., siRNA) or single stranded RNAs capable of folding back on themselves to form hairpin structures (e.g., shRNAs), the half-life of the therapeutic RNA(s) within the minicell is increased by use of minicell producing bacterial strains that harbor a deletion or other non-functional mutation in RNase genes (e.g., prokaryotic RNase III) responsible for the degradation of intracellular double stranded and/or hairpin RNA molecules.
  • RNase genes e.g., prokaryotic RNase III
  • the therapeutic RNA molecules In the absence of the RNase, the therapeutic RNA molecules accumulate to a higher level, increasing the potency of targeted minicells delivering the therapeutic nucleic acid molecules.
  • mutation or deletions are introduced into the rnc gene, which encodes for the only known somatic RNaseIII in this species.
  • Recombinantly expressed therapeutic, immunomodulatory, and immunogenic polypeptides to be delivered by targeted minicells include but are not limited to protein toxins, cholesterol-dependent cytolysins, functional enzymes, activated caspases, pro-caspases, cytokines, chemokines, cell-penetrating peptides, vaccine antigens, and any combination of the preceding examples, including conjugates thereof with molecules designed to modulate polarity and/or extend half-life (for example lipids or polyethylene glycol).
  • Recombinant expression of a polypeptide(s) can be the result of expression from any of the various episomal recombinant prokaryotic expression vectors known in the art including but not limited to plasmids, cosmids, phagemids, and bacterial artificial chromosomes (BACs), and any combination of the preceding examples.
  • recombinant expression can be achieved by a chromosomally located prokaryotic expression cassette present in one or more copies of the minicell-producing parent cell chromosome.
  • the delivery of protein toxins using the targeted minicells of the present application is an advantageous approach in applications where selective elimination of cells in vivo is desirable.
  • Protein toxins which can facilitate endosomal delivery of payloads and/or function as toxic payloads include, but are not limited to, fragments A/B of diphtheria toxin, fragment A of diphtheria toxin, anthrax toxins LF and EF, adenylate cyclase toxin, gelonin, botulinolysin B, botulinolysin E3, botulinolysin C, botulinum toxin, cholera toxin, clostridium toxins A, B and alpha, ricin, shiga A toxin, shiga-like A toxin, cholera A toxin, pertussis S1 toxin, perfringolysin O, Pseudomonas exotoxin A, E.
  • LTB heat labile toxin
  • melittin pH stable variants of listeriolysin O (pH-independent; amino acid substitution L461T)
  • thermostable variants of listeriolysin O amino acid substitutions E247M, D320K
  • pH and thermostable variants of listeriolysin O amino acid substitutions E247M, D320K, and L461T
  • streptolysin O streptolysin O c, streptolysin O e, sphaericolysin, anthrolysin O, cereolysin, thuringiensilysin O, weihenstephanensilysin, alveolysin, brevilysin, butyriculysin, tetanolysin O, novyilysin, lectinolysin, pneumolysin, mitilysin, pseudopneumolysin, suilysin, intermedilysin
  • Cytokines may be recombinantly expressed in and delivered by minicells to impart therapeutic and immunomodulatory effects.
  • Cytokines that may be expressed in and delivered by minicells include but are not limited to Granulocyte Macrophage Colony Stimulating Factor (GMCSF), Tumor Necrosis Factor Alpha (TNF- ⁇ ), Interferon Gamma (IFN- ⁇ ), Interferon Alpha 2b (IFN- ⁇ 2b), Interleukin-2 (IL-2), Interleukin-1a (IL-1a), Interleukin-12 (IL-12), and TRAIL.
  • Vaccine antigens that may be recombinantly expressed and delivered include but are not limited to those encoded for in the genomes of bacterial, viral, and parasitic organisms.
  • Vaccine antigens that may be recombinantly expressed and delivered also include those antigens and neo-antigens present on cancer cells including but not limited to Carcinogenic Embryonic Antigen (CEA), Mesothelin, Mucin-1 (MUC1), BAGE, GAGE, MAGE, SSX, EGFRvIII, Her-2, Gp100, Melan-A/Mart-1, Tyrosinase, PSA, Mammaglobin-A, p53, livin, survivin, beta-catenin-m, HSP70-2/m, HLA-A2-R170J, WT1, PR1, E75, ras, AFP, URLC10, mutant p53, and NY-ESO-1.
  • CEA Carcinogenic Embryonic Antigen
  • MUC1 Mucin-1
  • BAGE GAGE
  • MAGE MAGE
  • MAGE SSX
  • EGFRvIII Her-2
  • Gp100 Melan-A/Mart
  • Polypeptides can be localized to different sub-cellular compartments of the minicell at the discretion of the skilled artisans.
  • targeted minicells disclosed herein are derived from a Gram-negative parental minicell-producing strain, recombinantly expressed polypeptides produced therefrom can be localized to the cytosol, the inner leaflet of the inner membrane, the outer leaflet of the inner membrane, the periplasm, the inner leaflet of the outer membrane, the outer membrane of minicells, and any combination of the proceeding.
  • targeted minicells disclosed herein are derived from a Gram-positive parental minicell-producing strain
  • recombinantly expressed therapeutic polypeptides produced therefrom can be localized to the cytosol, the cell wall, the inner leaflet of the membrane, the membrane of minicells, and any combination of the proceeding.
  • the polypeptide payload(s) is pre-formed by the parental cell by way of recombinant expression from a prokaryotic expression cassette (either chromosomal or episomal in location) and is then packaged inside of the minicells as the payload, the half-life of the polypeptide payload(s) within the minicell is increased by use of minicell producing bacterial strains that harbor a deletion or other non-functional mutation in protease genes (e.g., the lon protease of E. coli ) responsible for proteolysis.
  • protease genes e.g., the lon protease of E. coli
  • the polypeptide payload(s) molecule(s) In the absence of the protease(s), the polypeptide payload(s) molecule(s) accumulates to a higher level, increasing the potency of targeted minicells delivering the polypeptide payload molecules.
  • mutation or deletions can be introduced into one or more of the lon, tonB, abgA, ampA, ampM, pepP, clpP, dcp, ddpX/vanX, elaD, frvX, gcp/b3064, hslV, hchA/b1967, hyaD, hybD, hycH, hycI, iadA, ldcA, ycbZ, pepD, pepE, pepQ, pepT, pmbA, pqqL, prlG, ptrB, sgcX, sprT, tldD,
  • Effective delivery of therapeutic, immunomodulatory, and immunogenic polypeptides and nucleic acid payloads by way of receptor mediated endocytosis can be limited if the polypeptide(s) and/or nucleic acid(s) delivered are exposed to the protease and nuclease rich environment of the endosomal compartment for too long prior to being released to the cytosol of the targeted eukaryotic cell. Most polypeptides and nucleic acids have no intrinsic ability to escape the endosomal compartment. A few exceptions from the protein toxin family, including the cholesterol dependent cytolysins/toxins (e.g.
  • LLO perfringolysin O
  • SLO streptolysin O
  • fragment A/B of diphtheria toxin escape mediated by fragment B
  • ricin ricin
  • Pseudomonas exotoxin A Those protein toxins that do contain intrinsic endosomal escape properties do not necessarily require the co-presence of a separate endosomal disruption component in the targeted minicell to be effective and the decision to include an endosomal disrupting agent is at the discretion of the skilled artisans.
  • LLO listeriolysin O
  • Listeria monocytogenes are capable of being incorporated into those embodiments of the present application that include but are not limited to a polypeptide or nucleic acid payload component or other therapeutic payload requiring endosomal escape to confer best activity.
  • full length LLO (containing the signal secretion sequence) is used as the endosomal disruption agent.
  • the signal sequence of LLO (making cLLO) is removed at the genetic level using recombinant techniques known in the art and cLLO is used as the endosomal disruption agent.
  • thermostable and/or pH-independent versions of LLO (harboring mutations E247M, D320K and/or L461T, sLLOpH) are employed.
  • LLO or any of the LLO variants or other endosomal escape facilitators
  • receptor mediated endocytosis carries the minicell into the endosome.
  • the harsh environment of the endosome begins to degrade the engulfed minicell, co-releasing the payload(s) along with the endosomal disruption agent (e.g., LLO, any of its variants, or other endosomal disrupting agent).
  • the released endosomal disruption agent component then facilitates release of the payload(s) from the endosome into the cytosol where the payload can exert its biological effect(s).
  • preferred endosomal disruption agents include other cytolysins, such as PFO and SLO and derivatives thereof, and phospholipases, such as PI-PLC or PC-PLC.
  • minicells disclosed herein can also be used as targeted immunogenic minicell vaccines.
  • Protein antigen and/or DNA vaccine loaded minicells are targeted directly to distinct subsets of antigen presenting cells of the immune system by utilizing antibodies or other minicell-surface displayed molecules that are specific for eukaryotic cell surface markers expressed by these antigen presenting cell subsets.
  • targeted vaccine minicells are further engineered to either express or be loaded with exogenous adjuvant as deemed appropriate by the skilled artisan.
  • Adjuvants can be general adjuvants (such as Keyhole limpet hemocyanin or complete Freud's adjuvant) or can be targeted molecular adjuvants.
  • Targeted molecular adjuvants include those that are antagonists or agonists of Toll-Like Receptors as well as other cellular constituents that have immunomodulatory properties.
  • Targeted vaccines provide recipient immunity to infectious disease agents including but not limited to those infectious disease agents of bacterial, viral, and parasitic origin(s).
  • Targeted vaccines also provided recipient immunity to tumors and other aberrant disease(s) of autologous nature.
  • minicell compositions are formulated into a pharmaceutical composition, filled into sterile pharmaceutical grade containers, stoppered, sealed, and subjected to terminal sterilization by irradiation.
  • compositions including but not limited to, pharmaceutical compositions.
  • pharmaceutical composition used herein refers to a mixture comprising at least one excipient, preferably a physiologically acceptable excipient, and one or more minicell compositions.
  • the pharmaceutical composition may further include one or more “diluents” or “carriers”.
  • excipient refers to a chemical compound or combination of compounds that does not inhibit or prevent the incorporation of the biologically active peptide(s) into cells or tissues.
  • An excipient is any more or less inert substance that can be added to a composition in order to confer a suitable property, for example, a target concentration of active, suitable consistency, stability and/or to achieve properties in which delivery of the active to the target is facilitated (e.g. a drug formulation).
  • D-trehalose in sterile water.
  • D-trehalose in sterile water.
  • the preferred concentration of D-trehalose is 12% (w/v) and the preferred diluent is sterile water.
  • a “diluent” is a pharmaceutically acceptable solvent, for example an aqueous solvent that facilitates dissolution of the composition in the solvent, and it may also serve to stabilize the biologically active form of the composition or one or more of its components.
  • Salts dissolved in water to make buffered solutions are utilized as diluents in the art and preferred diluents are buffered solutions containing one or more different salts.
  • An non-limiting example of preferred buffered solution is phosphate buffered saline (particularly in conjunction with compositions intended for pharmaceutical administration), as it mimics the salt conditions of human blood, although buffered solutions may also be prepared and used at extremes in pH, depending on the route of administration, buffer capacity, and volume of the product administered. Since buffer salts can control the pH of a solution at low concentrations, a buffered diluent rarely modifies the biological activity of a given compound or pharmaceutical composition.
  • a “carrier” as used herein is an inert substance that allows an active ingredient to be formulated or compounded into a suitable dosage form [e.g., microparticle (e.g., a microsphere), pill, capsule, tablet, solution, colloid, suspension, emulsion, film, gel, cream, ointment; paste, etc.].
  • a “physiologically acceptable carrier” is a compound suitable for use under physiological conditions that does not abrogate (reduce, inhibit, or prevent) the biological activity and properties of the compound.
  • the carrier is a physiologically acceptable carrier, preferably a pharmaceutically or veterinarily acceptable carrier, in which the minicell composition is disposed.
  • a “pharmaceutical composition” refers to a composition wherein the excipient is a pharmaceutically acceptable excipient, while a “veterinary composition” is one wherein the excipient is a veterinarily acceptable excipient.
  • pharmaceutically acceptable excipient or “veterinarily acceptable excipient” used herein includes any medium or material that is not biologically or otherwise undesirable, i.e., the excipient may be administered to an organism along with a minicell composition without causing any undesirable biological effects or interacting in a deleterious manner with the complex or any of its components or the organism.
  • therapeutically effective amount refers to an amount sufficient to induce or effectuate a therapeutic response in the target cell, tissue, or body of an organism. What constitutes a therapeutically effective amount will depend on a variety of factors, which the knowledgeable practitioner will take into account in arriving at the desired dosage regimen.
  • disintegrating agents can also be included, such as cross-linked polyvinyl pyrrolidone, agar, or alginic acid or a salt thereof such as sodium alginate.
  • suitable excipients and carriers include hydrogels, gellable hydrocolloids, and chitosan. Chitosan microspheres and microcapsules can be used as carriers.
  • WO 98/52547 which describes microsphere formulations for targeting compounds to the stomach, the formulations comprising an inner core (optionally including a gelled hydrocolloid) containing one or more active ingredients, a membrane comprised of a water insoluble polymer (e.g., ethylcellulose) to control the release rate of the active ingredient(s), and an outer layer comprised of a bioadhesive cationic polymer, for example, a cationic polysaccharide, a cationic protein, and/or a synthetic cationic polymer; U.S. Pat. No. 4,895,724.
  • a bioadhesive cationic polymer for example, a cationic polysaccharide, a cationic protein, and/or a synthetic cationic polymer
  • chitosan is cross-linked using a suitable agent, for example, glutaraldehyde, glyoxal, epichlorohydrin, and succinaldehyde.
  • a suitable agent for example, glutaraldehyde, glyoxal, epichlorohydrin, and succinaldehyde.
  • Compositions employing chitosan as a carrier can be formulated into a variety of dosage forms, including pills, tablets, microparticles, and microspheres, including those providing for controlled release of the active ingredient(s).
  • bioadhesive cationic polymers include acidic gelatin, polygalactosamine, polyamino acids such as polylysine, polyhistidine, polyornithine, polyquaternary compounds, prolamine, polyimine, diethylaminoethyldextran (DEAE), DEAE-imine, DEAE-methacrylate, DEAE-acrylamide, DEAE-dextran, DEAE-cellulose, poly-p-aminostyrene, polyoxethane, copolymethacrylates, polyamidoamines, cationic starches, polyvinylpyridine, and polythiodiethylaminomethylethylene.
  • polyamino acids such as polylysine, polyhistidine, polyornithine, polyquaternary compounds
  • prolamine polyimine, diethylaminoethyldextran (DEAE), DEAE-imine, DEAE-methacrylate, DEAE-acrylamide, DEAE-dextran,
  • minicell compositions can be uniformly (homogeneously) or non-uniformly (heterogeneously) dispersed in the carrier.
  • Suitable formulations of minicell composition include, but are not limited to, colloidal solution, dry powder, frozen suspension, liquid suspension and lyophilized formulations.
  • Dry formulations include freeze dried and lyophilized powders, which are particularly well suited for aerosol delivery to the sinuses or lung, or for long term storage followed by reconstitution in a suitable diluent prior to administration.
  • Other preferred dry formulations include those wherein a composition disclosed herein is compressed into tablet or pill form suitable for oral administration or compounded into a sustained release formulation.
  • the formulation be encapsulated with an enteric coating to protect the formulation and prevent premature release of the minicell compositions included therein.
  • the compositions disclosed herein can be placed into any suitable dosage form. Pills and tablets represent some of such dosage forms.
  • the compositions can also be encapsulated into any suitable capsule or other coating material, for example, by compression, dipping, pan coating, spray drying, etc. Suitable capsules include those made from gelatin and starch. In turn, such capsules can be coated with one or more additional materials, for example, and enteric coating, if desired.
  • Liquid formulations include aqueous formulations, gels, and emulsions.
  • compositions that comprise a bioadhesive, preferably a mucoadhesive, coating.
  • a “bioadhesive coating” is a coating that allows a substance (e.g., a minicell composition) to adhere to a biological surface or substance better than occurs absent the coating.
  • a “mucoadhesive coating” is a preferred bioadhesive coating that allows a substance, for example, a composition to adhere better to mucosa occurs absent the coating.
  • minicells can be coated with a mucoadhesive. The coated particles can then be assembled into a dosage form suitable for delivery to an organism.
  • the dosage form is then coated with another coating to protect the formulation until it reaches the desired location, where the mucoadhesive enables the formulation to be retained while the composition interacts with the target cell surface transport moiety.
  • compositions disclosed herein can be administered to any organism, preferably an animal, preferably a mammal, bird, fish, insect, or arachnid.
  • Preferred mammals include bovine, canine, equine, feline, ovine, and porcine animals, and non-human primates. Humans are particularly preferred.
  • Multiple techniques of administering or delivering a compound exist in the art including, but not limited to, ocular, aural, buccal, oral, rectal, (e.g. an enema or suppository), vaginal, transurethral, nasal, pulmonary, parenteral, and topical administration.
  • sufficient quantities of the biologically active peptide are delivered to achieve the intended effect.
  • composition to be delivered will depend on many factors, including the effect to be achieved, the type of organism to which the composition is delivered, delivery route, dosage regimen, and the age, health, and sex of the organism. As such, the particular dosage of a composition incorporated into a given formulation is left to the ordinarily skilled artisan's discretion.
  • compositions disclosed herein are administered as agents to achieve a particular desired biological result, which may include a therapeutic, diagnostic, or protective effect(s) (including vaccination), it may be possible to combine the minicell composition with a suitable pharmaceutical carrier.
  • suitable pharmaceutical carrier and the preparation of the minicells as a therapeutic or protective agent will depend on the intended use and mode of administration. Suitable formulations and methods of administration of therapeutic agents include but are not limited to those for oral, pulmonary, nasal, buccal, ocular, dermal, rectal, intravenous, intravesical, intrathecal, intracranial, intratumoral, pleural, or vaginal delivery.
  • the context-dependent functional entity can be delivered in a variety of pharmaceutically acceptable forms.
  • the context-dependent functional entity can be delivered in the form of a solid, suspension, solution, emulsion, dispersion, and the like, incorporated into a pill, capsule, tablet, suppository, aerosol, droplet, or spray. Pills, tablets, suppositories, aerosols, powders, droplets, and sprays may have complex, multilayer structures and have a large range of sizes. Average sizes of aerosols, powders, droplets, and sprays may range from small (submicron) to large ( ⁇ 200 micron) in size.
  • compositions disclosed herein can be used in the form of a solid, a lyophilized powder, a solution, an emulsion, a dispersion, and the like, wherein the resulting composition contains one or more of the compounds disclosed herein, as an active ingredient, in admixture with an organic or inorganic carrier or excipient suitable for enteral or parenteral applications.
  • the active ingredient may be compounded, for example, with the usual non-toxic, pharmaceutically acceptable carriers for tablets, pellets, capsules, suppositories, solutions, emulsions, suspensions, and any other form suitable for use.
  • excipients which can be used include glucose, lactose, mannose, gum acacia, gelatin, mannitol, trehalose, starch paste, magnesium trisilicate, talc, corn starch, keratin, colloidal silica, potato starch, urea, medium chain length triglycerides, dextrans, and other carriers suitable for use in manufacturing preparations, in solid, semisolid, or liquid form.
  • auxiliary, stabilizing, thickening, flavoring and coloring agents may be used.
  • a stabilizing agent include trehalose, preferably at concentrations of 0.1% or greater (See, e.g., U.S. Pat. No. 5,314,695).
  • the active compound is included in the pharmaceutical composition in an amount sufficient to produce the desired effect upon the process or condition of diseases.
  • ionizing irradiation include gamma irradiation, high frequency electromagnetic irradiation, E-beam (electron beam, beta irradiation) irradiation, X-ray (photon) irradiation, and UV irradiation.
  • gamma irradiation high frequency electromagnetic irradiation
  • E-beam electron beam, beta irradiation
  • X-ray (photon) irradiation X-ray (photon) irradiation
  • UV irradiation One of the preferred type of ionizing irradiation for use in the methods and compositions disclosed herein is gamma irradiation.
  • the dose of ionizing irradiation suitable for use in the methods and compositions disclosed herein can vary.
  • the dose of ionizing irradiation required for reducing parental cell and adventitious microbial bioburden(s) to acceptable standards of sterility can be empirically determined.
  • Non-limiting exemplary range of the irradiation dose is between 5 kGy and 40 kGy, for example the irradiation can be at a dose of, or at a dose of about, 5 kGy, 8 kGy, 10 kGy, 11 kGy, 12 kGy, 13 kGy, 14 kGy, 15 kGy, 16 kGy, 17 kGy, 18 kGy, 19 kGy, 20 kGy, 21 kGy, 22 kGy, 23 kGy, 24 kGy, 25 kGy, 28 kGy, 30 kGy, 35 kGy, 40 kGy, or a range between any of these values.
  • the irradiation is at a dose of about 5 kGy to about 30 kGy, or about 10 kGy to about 25 kGy. In some embodiments, the irradiation is at a dose of 25 kGy.
  • the composition comprising minicells suitable for being irradiated for sterilization can be in various forms, including and not limited to, liquid suspension, frozen suspension, and freeze-dried lyophilized (lyophile) cake formulations.
  • the formulation for sterilization by ionizing irradiation for the composition comprising minicells is a frozen suspension or frozen lyophile.
  • terminal sterilization of the composition comprising minicells by ionizing irradiation comprises, or is, terminally sterilizing ionizing gamma irradiation at a dose of 25 kGy.
  • Sterility of a minicell-based biopharmaceutical product can be determined using methods known in the art, for example, as described in USP ⁇ 71> standards under version USP 38 NF 33.
  • sterility under USP ⁇ 71> is defined as no growth (turbidity compared to negative control) in Fluid Thioglycollate Medium (medium sterilized by a validated process) incubated at 32.5° C. ⁇ 2.5° C. over a 14-day span, post irradiation.
  • the minicell biopharmaceutical product is formulated in liquid of 1 mL or less, and entire vial is used to inoculate growth medium for sterility testing.
  • the number of containers to be tested in a given production lot under USP ⁇ 71> include, if less than 100 containers, 10% or 4 containers, whichever is greatest. If greater than 100 containers but fewer than 500, 10 containers are to be used. If more than 500 containers, 2% or 20 containers, whichever is less. For ophthalmic and other non-injectable biopharmaceutical products, if not more than 200 containers, 5% or 2 containers, whichever is greater. If more than 200 containers, 10 containers are required to be tested.
  • the present application relates to minicell-based biopharmaceutical agents designed to be effective against cancer(s), infectious disease(s), genetic disorder(s), autoimmune condition(s), and other maladies.
  • Solid tumors include, but are not limited to, solid tumors, metastatic tumors, and liquid tumors.
  • Solid and metastatic tumors include those of epithelial, fibroblast, muscle and bone origin and include but are not limited to breast, lung, pancreatic, prostatic, testicular, ovarian, gastric, intestinal, mouth, tongue, pharynx, hepatic, anal, rectal, colonic, esophageal, urinary bladder, gall bladder, skin, uterine, vaginal, penal, and renal cancers.
  • Other solid cancer types that may be treated with the minicells disclosed herein include but are not limited to adenocarcinomas, sarcomas, fibrosarcomas, and cancers of the eye, brain, and bone.
  • Liquid tumors that can be treated by the minicells disclosed herein include but are not limited to non-Hodgkin's lymphoma, myeloma, Hodgkin's lymphoma, acute lymphocytic leukemia, chronic lymphocytic leukemia, acute myeloid leukemia, chronic myeloid leukemia, and other leukemias.
  • Infectious disease(s) can be treated prophylactically using immunogenic minicells or targeted minicell vaccine compositions by immunizing a subject prior to its next exposure to the infectious agent against which said vaccine is intended to prevent.
  • a therapeutic vaccine may be given to a subject currently suffering from disease caused by the infectious agent that the vaccine is intended to prevent.
  • Infectious disease(s) include but are not limited to those of bacterial, viral, fungal, and parasitic origin.
  • Bacterial pathogens against which immunogenic minicells and targeted vaccine minicells are designed to prevent include but are not limited to Escherichia spp., Salmonella spp., Shigella spp., Vibrio spp., Neisseria spp., Campylobacter spp., Pseudomonas spp., Yersinia spp., Chlamydia spp., Acinetobacter spp., Listeria spp., Bacillus spp., Haemophilus spp., Clostridium spp., Francisella spp., Rickettsia spp., and others.
  • Immunogenic minicells and targeted minicell vaccines against these agents can be generated from minicells derived from minicell-producing pathogenic strains or from minicells derived from non-pathogenic strains but engineered to recombinantly express or produce a heterologous antigen(s) from a pathogenic strain.
  • Viral pathogens against which immunogenic minicells and targeted vaccine minicells are designed to prevent include but are not limited to all strains and sub-strains of influenza, parainfluenza, human immunodeficiency virus, Epstein Barr virus, Respiratory Syncitial virus, Varicella zoster, human papilloma virus, hepatitis A virus, hepatitis B virus, hepatitis C virus, dengue fever virus, yellow fever virus, west nile virus, MERS virus, SARS virus, coxsackie virus, herpes simplex virus, cytomegalovirus, rabies virus, and others.
  • Fungal pathogens against which immunogenic minicells and targeted vaccine minicells are designed to prevent include but are not limited to Candida spp., Aspergillus spp., Cryptococcus spp., Histoplasma spp., Pneumocystis spp., Stachybotrys spp., and others.
  • Parasitic pathogens against which immunogenic minicells and targeted vaccine minicells are designed to prevent include but are not limited to Acanthamoeba, Ascaris lumbricoides, Balantidium coli, Cochliomyia hominivorax, Entamoeba histolytica, Fasciola hepatica, Giardia lamblia, Leishmania, Loa loa, Plasmodium falciparum, Schistosoma, Strongyloides stercoralis, Toxoplasma gondii, Trypansoma, Wuchereria bancrofti , and others.
  • Minicell-based biopharmaceuticals that have been terminally sterilized by exposure to ionizing irradiation and are intended to treat or otherwise prevent against the disease types and infectious agents listed above may be administered to a subject parenterally or topically.
  • Parenteral routes of administration require injection and include but are not limited to intravenous, intravitreal, intrathecal, intraperitoneal, intratumoral, intramuscular and subcutaneous routes of administration.
  • Topical routes of administration include but are not limited to intravesical, intrarectal, vaginal, mucosal, aural, oral, nasal, pulmonary, intrapleural (through a pleural catheter), and dermal routes of administration.
  • Some embodiments disclosed herein relate to creating an optimized strain and preparing targeted therapeutic, immunodulatory, and immunogenic minicells from, but not limited to, the bacterial family Enterobacteriaceae; formulating said minicells into a pharmaceutical composition; filling into sterile vials or syringes; sealing, and terminally sterilizing the minicell-based pharmaceutical composition by exposure to ionizing irradiation.
  • a pharmaceutical composition comprising a plurality of bacterial minicells, wherein the bacterial minicells and/or the pharmaceutical composition have been exposed to ionizing irradiation.
  • the pharmaceutical composition can, for example, comprise one or more pharmaceutically acceptable excipient or a pharmaceutically acceptable diluent.
  • the pharmaceutically acceptable excipient can be, for example, trehalose (e.g., trehalose in diluent).
  • the pharmaceutically acceptable diluent can be, for example, sterile water (e.g., sterile water for injection).
  • the pharmaceutical composition and/or the plurality of bacterial cells contained therein have been terminally sterilized.
  • the pharmaceutical composition is sterile.
  • the pharmaceutical composition can contain viable microbial contaminants at a level conforming to USP ⁇ 71> standards under version USP 38 NF 33.
  • the level of viable microbial contaminants in the pharmaceutical composition that has been exposed to ionizing irradiation can be, for example, less than 1 ⁇ 10 8 colony forming units (CFU) per mL, less than 1 ⁇ 10 7 CFU per mL, less than 1 ⁇ 10 6 CFU per mL, less than 1 ⁇ 10 5 CFU per mL, less than 1 ⁇ 10 4 CFU per mL, less than 1 ⁇ 10 3 CFU per mL, less than 1 ⁇ 10 2 CFU per mL, less than 10 CFU per mL, or less than 1 CFU per mL.
  • CFU colony forming units
  • the level of viable microbial contaminants in the pharmaceutical composition that has been exposed to ionizing irradiation can be, or can be about, 1 ⁇ 10 8 CFU per mL, 5 ⁇ 10 7 CFU per mL, 1 ⁇ 10 7 CFU per mL, 5 ⁇ 10 6 CFU per mL, 1 ⁇ 10 6 CFU per mL, 5 ⁇ 10 5 CFU per mL, 1 ⁇ 10 5 CFU per mL, 5 ⁇ 10 4 CFU per mL, 1 ⁇ 10 4 CFU per mL, 5 ⁇ 10 3 CFU per mL, 1 ⁇ 10 3 CFU per mL, 5 ⁇ 10 2 CFU per mL, 1 ⁇ 10 2 CFU per mL, 50 CFU per mL, 10 CFU per mL, 5 CFU per mL, 1 CFU per mL, or a range between any two of these values.
  • the level of minicell-producing viable microbial contaminants contamination in the pharmaceutical composition following exposure to ionizing irradiation can be, for example, less than 1 in 10 2 minicells, less than 1 in 10 3 minicells, less than 1 in 10 4 minicells, less than 1 in 10 5 minicells, less than 1 in 10 6 minicells, less than 1 in 10 7 minicells, less than 1 in 10 8 minicells, less than 1 in 10 9 minicells, less than 1 in 10 10 minicells, less than 1 in 10 11 minicells, less than 1 in 10 12 minicells, less than 1 in 10 13 minicells, less than 1 in 10 14 minicells, less than 1 in 10 15 minicells, or less than 1 in 10 16 minicells.
  • the types, genotypes and phenotypes of the minicells comprised in the pharmaceutical can vary.
  • said bacterial minicells express and/or display invasin or a functional equivalent thereof on their surfaces.
  • the invasin can be, but is not limited to, an invasin from Yersinia pseudotuberculosis .
  • the bacterial minicells can, for example, comprise perfringolysin O (PFO).
  • PFO perfringolysin O
  • the bacterial minicells express and/or displays invasin or a functional equivalent thereof on their surfaces, and comprise PFO.
  • the level of minicell-producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 5 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 6 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 7 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 8 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 9 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 10 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 11 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 12 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 13 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 14 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 15 minicells.
  • the level of minicell producing viable parental cell contamination in the pharmaceutical composition following exposure to ionizing irradiation is less than 1 in 10 16 minicells.
  • the pharmaceutical composition comprising the minicells is devoid of growth in Liquid Thioglycollate Medium after, or after about, 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days, 15 days, 16 days, 17 days, 18 days, 19 days, 20 days, or a range between any two of these values, at, for example, 32.5° C. ⁇ 2.5° C.
  • a minicell-based biopharmaceutical product following exposure to ionizing irradiation, is devoid of growth in Liquid Thioglycollate Medium after 14 days at 32.5° C. ⁇ 2.5° C. and therefore is sterile as per the definition of USP ⁇ 71> standards under version USP 38 NF 33.
  • VAX014 Minicell Properties in a Frozen Suspension Following Exposure to Ionizing Gamma Irradiation at Doses of 5, 15 and 25 kGy
  • VAX-IP VAX014 minicell properties following exposure to ionizing gamma irradiation in a frozen suspension at doses of 5, 15 and 25 kGy.
  • VAX014 minicells (contains both Invasin and Perfringolysin O) were made from parental strain VAX20B9, a recombinant Escherichia coli K-12 minicell-producing strain harboring the L-rhamnose-inducible bacterial expression plasmid, pVX-336 (containing a transcriptional fusion between Invasin and Perfringolysin O under control of the pRHA BAD promoter).
  • VAX20B9 research cell bank was thawed at room temperature and the entire vial contents used to inoculate a 1 L starter culture in Soytone-based MSB-NaCl media containing kanamycin (50 ⁇ g/mL), diaminopimelic acid (100 ⁇ g/mL), lysine (55 ⁇ g/mL), and 0.2% D-glucose.
  • the starter culture was grown for 18 hours at 30° C. and the following day, 200 mL used to inoculate 14 L of identical media, without D-glucose.
  • the final minicell fractions were concentrated by (TFF), then pelleted by high-speed centrifugation (20 min at 11,000 ⁇ g) and the final VAX014 minicell pellets resuspended in 12% sterile D-trehalose in pharmaceutical grade water at a concentration of 3.33 ⁇ 10 10 VAX014 minicells per milliliter to make bulk drug substance.
  • 100 ⁇ L of bulk drug substance was plated on Soytone-based MSB-NaCl solid agar medium containing diaminopimelic acid (100 ⁇ g/mL) and lysine (55 ⁇ g/mL) and allowed to grow overnight at 30° C.
  • VAX014 drug substance was then vialed (3 mL per vial—1 ⁇ 10 11 VAX014 minicells per vial) into 5 mL clear serum vials using a semi-automated hand-fill, and each vial stoppered and sealed. Vialed VAX014 drug substance was then exposed to one of three irradiation doses (5, 15, or 25 kGy, 25 vials irradiated at each dose level) while frozen.
  • VAX014 drug product On Day 7 post-irradiation, 3 randomly selected vials were thawed at room temperature and VAX014 drug product characterized using a battery of characterization tests including concentration uniformity, appearance, container closure integrity, visual inspection, pH testing, microscopic evaluation of product aggregation and presence of particulate matter, determination of the amount of Invasin on the VAX014 minicell surface by FACS using a monoclonal antibody against Invasin, the hemolytic activity of Perfringolysin O on whole citrated sheep blood, cell killing potency of VAX014 against HTB-9 human urothelial carcinoma cells, and the final viable colony forming unit counts as a measure of the reduction in bioburden from non-irradiated material.
  • compositions comprising minicells before and after gamma irradiation FORMULATION: Frozen Suspension VAX014 (1 ⁇ 10 11 ) in 3 mL 12% sterile D-Trehalose DOSE PROPERTY 0 5 kGy 15 kGy 25 kGy Glass Color (VI) Clear Brown Slightly Much Darker Darker Brown Brown Stopper intact (VI) Y Y Y Y Seal intact (VI) Y Y Y Y Change in DS appearance (VI) N N N N N Precipitates (MI) N N N N N Aggregates (MI) ⁇ 5% ⁇ 5% ⁇ 5% ⁇ 5% OD600 1.86 2.06 1.99 2.02 FACS against Invasin (% 83.6 86.9 88.9 89.4 positive) PFO hemolytic activity 34.6 32.6 36.1 40.6 (PFO ng/10 8 mcs) Potency (cell killing - 41.31 46.16 47.21 49.27 immediate) (VAX-
  • VAX014 Minicell Properties in a Frozen Lyophile Following Exposure to Ionizing Gamma Irradiation at Doses of 5, 15 and 25 kGy
  • VAX-IP VAX014 minicell properties following exposure to ionizing gamma irradiation in a frozen lyophile at doses of 5, 15 and 25 kGy.
  • VAX014 minicells (contains both Invasin and Perfringolysin O) are made from parental strain VAX20B9, a recombinant Escherichia coli K-12 minicell-producing strain harboring the L-rhamnose-inducible bacterial expression plasmid, pVX-336 (contains a transcriptional fusion between Invasin and Perfringolysin O under control of the pRHA BAD promoter).
  • VAX20B9 research cell bank was thawed at room temperature and the entire vial contents used to inoculate a 1 L starter culture in Soytone-based MSB-NaCl media containing kanamycin (50 ⁇ g/mL), diaminopimelic acid (100 ⁇ g/mL), lysine (55 ⁇ g/mL), and 0.2% D-glucose.
  • the starter culture was grown for 18 hr at 30° C. and the following day, 200 mL used to inoculate 14 L of identical media, without D-glucose.
  • the final minicell fractions were concentrated by (TFF), then pelleted by high-speed centrifugation (20 min at 11,000 ⁇ g) and the final VAX014 minicell pellets resuspended in 12% sterile D-trehalose in pharmaceutical grade water at a concentration of 3.33 ⁇ 10 10 VAX014 minicells per milliliter to make bulk drug substance.
  • 100 ⁇ L of bulk drug substance was plated on Soytone-based MSB-NaCl solid agar medium containing diaminopimelic acid (100 ⁇ g/mL) and lysine (55 ⁇ g/mL) and allowed to grow overnight at 30° C.
  • VAX014 drug substance was then vialed (3 mL per vial—1 ⁇ 10 11 VAX014 minicells per vial) into 5 mL clear serum vials using a semi-automated hand-fill, and each vial stoppered with a NovaPure lyophilization compatible stopper. Vial contents were lyophilized and then overseals applied. Vialed, lyophilized VAX014 drug substance was then exposed to one of three irradiation doses (5, 15, or 25 kGy, 25 vials irradiated at each dose level) while frozen.
  • VAX014 drug product On Day 7 post-irradiation, 3 randomly selected vials were thawed at room temperature and VAX014 drug product characterized using a battery of characterization tests including concentration uniformity, appearance, container closure integrity, visual inspection, pH testing, microscopic evaluation of product aggregation and presence of particulate matter, determination of the amount of Invasin on the VAX014 minicell surface by FACS using a monoclonal antibody against Invasin, the hemolytic activity of Perfringolysin O on whole citrated sheep blood, cell killing potency of VAX014 against HTB-9 human urothelial carcinoma cells, and the final viable colony forming unit counts as a measure of the reduction in bioburden from non-irradiated material. No changes in product integrity, stability, characteristics, and potency were observed, while the bioburden was reduced to zero at each dose level.
  • compositions comprising minicells before and after gamma irradiation FORMULATION: Frozen Lyophile VAX014 (1 ⁇ 10 11 ) lyophilized from 3 mL 12% sterile D-Trehalose DOSE PROPERTY 0 5 kGy 15 kGy 25 kGy Glass Color (VI) Clear Brown Slightly Much Darker Darker Brown Brown Stopper intact (VI) Y Y Y Y Seal intact (VI) Y Y Y Y Change in DS N N N N N appearance (VI) Precipitates (MI) N N N N N Aggregates (MI) ⁇ 5% ⁇ 5% ⁇ 5% ⁇ 5% OD600 1.60 1.62 1.73 1.71 FACS against Invasin 86.7 83.6 89.5 88.9 (% positive) PFO hemolytic activity 34.9 29.4 28.8 37.9 (PFO ng/10 8 mcs) Potency (cell killing - 50.87 56.55 49.7 51.56 immediate) (VA
  • FIGS. 2A-B show the results of the initial visual inspection, held at the vial level, post-irradiation. It was found that vials were darkened with increasing irradiation dose level, yet there was no visual loss of product (including volume and drug substance).
  • FIG. 2A shows sealed vials and FIG. 2B shows vials where the seals have been removed and the stoppers remain intact upon visual inspection. No macroscopic abnormalities were observed in the over-seal or stopper.
  • FIG. 3 further shows that there was no change in appearance (including color, consistency, and opaqueness) per secondary visual inspection of irradiated VAX014 drug product when removed from vials as compared to non-irradiated controls. Lyophiles were reconstituted in 3 mL of sterile water for injection prior to visual inspection.
  • irradiated and non-irradiated minicells were treated with EDTA and lysozyme, followed by osmotic shock to generate whole minicell lysates, each of which was then titrated against a fixed number of sheep red blood cells for 1 hour at 37° C. while shaking. Following a 1 hour co-incubation, red blood cells (RBCs) were pelleted and the supernatants removed and evaluated for hemoglobin release as a measure of hemolytic activity.
  • a standard curve using recombinant PFO was generated in parallel and used to calculate the concentration of Perfringolysin O in 1 ⁇ 10 8 VAX014 minicells. Therefore, there was no loss of perfringolysin O (protein toxin) activity in VAX014 minicell frozen suspension or frozen lyophiles after exposure to increasing amounts of ionizing gamma irradiation.
  • Potency of the minicells following gamma irradiation was also evaluated using a cell-killing potency assay against HTB-9 human urothelial carcinoma cells as compared to non-irradiated controls.
  • Vials of irradiated and non-irradiated VAX014 minicells were thawed at room temperature and immediately titrated against a fixed number of HTB-9 cells to generate EC 50 curves (0 hour, FIG. 5A ).
  • thawed vials were allowed to remain at room temperature for 4 hr prior to addition to HTB-9 cells to demonstrate no loss of activity over this time frame at this temperature (4 hour in room temperature (RT), FIG. 5B ).
  • RT room temperature
  • bladders were rinsed once with 100 ⁇ L of sterile saline and then saline (vehicle control) or an equivalent number of either irradiated (25 kGy) or non-irradiated VAX014 minicells administered in a 50 ⁇ L volume as a single dose treatment.
  • Catheters were locked for a total 1 hour treatment exposure time, then removed, and animals allowed to recover. Animals were monitored twice weekly for 70 days and comparative survival curves evaluated as a measure of pharmacological efficacy. The results are summarized in FIG. 9 demonstrates no loss of VAX014 pharmacological activity in vivo
  • Minicells generated from an Escherichia coli K-12 strain (strain VAX8I3) with an inducible minicell phenotype were generated by growing this strain in Soytone-based MSB-NaCl media containing diaminopimelic acid (100 ⁇ g/mL) and lysine (55 ⁇ g/mL) at 30° C. until an OD 600 of 1.0 was reached. At that point, IPTG was added to induce for the minicell production phenotype and the culture allowed to continue growing overnight.
  • Minicells were harvested using differential centrifugation followed by two sequential rounds of linear density sucrose gradients. Following purification, minicells (3 ⁇ 10 12 ) were loaded with doxorubicin by co-incubation with doxorubicin at a concentration of 400 ⁇ g/mL/1.0 ⁇ 10 10 minicells overnight at room temperature while shaking. The following day, bi-specific antibodies were generated by coupling human EGFR-1-specific mouse monoclonal antibody mAb528 to a Protein A-purified polyclonal rabbit anti-minicell antibody reagent at a molar ratio of 1:1 using recombinant Protein A/G (Pierce, Thermo-Fisher). Antibodies were mixed in equimolar amount prior to addition of Protein A/G.
  • reaction mixtures were held at room temperature while gently shaking for 1 hr to make bi-specific antibodies.
  • Doxorubicin loaded minicells were washed twice by pelleting and resuspension in 980 ⁇ L of 1 ⁇ PBS and 20 ⁇ L of bi-specific antibody complex added and co-incubated for 1 hr at 4° C. while gently shaking.
  • doxorubicin loaded antibody-coated minicells were washed twice by pelleting and resuspended in 12% D-trehalose to a concentration of 3.33 ⁇ 10 10 /mL.
  • doxorubicin-loaded, EGFR-1 targeted minicells were aseptically hand-filled by a semi-automated process into 5 mL amber serum vials, stoppered, over-sealed and frozen. Vials of doxorubicin-loaded EGFR-1 targeted minicells were gamma irradiated at a dose of 25 kGy while frozen and subject to analysis in comparison to non-irradiated controls.
  • Doxorubicin retention was also monitored by fluorescence microscopy and macroscopic observation of minicell pellets before and after gamma irradiation at 25 kGy.
  • the potency of EGFR-1 targeted, doxorubicin-loaded minicells was evaluated before and after gamma irradiation by titration against A549 human non-small cell carcinoma cells (overexpressing EGFR-1). As shown in FIGS. 7A-F , no differences in potency as determined by EC 50 curves were observed in response to increasing levels of gamma irradiation.
  • EGFR-1 targeted minicells comprising a functional nucleic acid (plasmid DNA) following gamma irradiation of frozen suspensions was studied. Plasmid integrity was evaluated using PCR with primers specific for the plasmid construct in minicells and in comparison to a naked plasmid control (plasmid control purified directly from equivalent number of minicells).
  • the anti-EGFR-1 antibody, mAb528 was coupled to the surface of minicells using the same Protein A/G approach described above respect to FIGS. 7A-F and analyzed post irradiation for its presence on the minicell surface using the same flow cytometry approach and secondary Alexa Flour 388-conjugated goat anti-mouse polyclonal antibody reagent. As shown in FIGS. 8A-B , no loss in plasmid integrity or stability was observed after the minicell-containing frozen suspensions were exposed to gamma irradation.
  • a range includes each individual member.
  • a group having 1-3 articles refers to groups having 1, 2, or 3 articles.
  • a group having 1-5 articles refers to groups having 1, 2, 3, 4, or 5 articles, and so forth.

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WO2017024059A8 (en) 2017-06-08
KR102558941B1 (ko) 2023-07-21
KR20230111275A (ko) 2023-07-25
EP3331575A4 (en) 2019-03-27
KR102687638B1 (ko) 2024-07-22
JP2021059600A (ja) 2021-04-15
AU2016301302B2 (en) 2023-01-12
WO2017024059A1 (en) 2017-02-09
US20190282629A1 (en) 2019-09-19
JP2018522036A (ja) 2018-08-09
CN108348624A (zh) 2018-07-31
CN113577323A (zh) 2021-11-02
JP6824960B2 (ja) 2021-02-03
US11564953B2 (en) 2023-01-31

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